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Free Radic Biol Med. Author manuscript; available in PMC 2008 Apr 15.
Published in final edited form as:
Free Radic Biol Med. 2007 Apr 15; 42(8): 1193–1200.
Published online 2007 Jan 13. doi: 10.1016/j.freeradbiomed.2007.01.019
PMCID: PMC1931511
NIHMSID: NIHMS21064
PMID: 17382200

Mn PORPHYRIN-BASED SOD MIMIC, MnTE-2-PyP5+, TARGETS MOUSE HEART MITOCHONDRIA

Ivan Spasojevic,1,* Yumin Chen,2 Teresa J. Noel,2 Yiqun Yu,1 Marsha P. Cole,2 Lichun Zhang,1 Yunfeng Zhao,2 Daret K. St Clair,2 and Ines Batinic-Haberle3,*
Author information Copyright and License information PMC Disclaimer

Abstract

The Mn(III) meso-tetrakis(N-ethylpyridinium-2-yl)porphyrin, MnIIITE-2-PyP5+ (AEOL-10113) has proven effective in treating oxidative stress-induced conditions including cancer, radiation damage, diabetes, and central nervous system trauma. The ortho cationic pyridyl nitrogens of MnTE-2-PyP5+ are essential for its high antioxidant potency. The exceptional ability of MnIIITE-2-PyP5+ to dismute O2.− parallels its ability to reduce ONOO− and CO3−. Decreasing levels of all these reactive species is considered its predominant mode of action, that may also involve redox-regulation of signaling pathways. Recently, Ferrer-Sueta at al (Free Radic. Biol Med. 2006) showed, with submitochondrial particles, that ≥ 3 μM MnIIITE-2-PyP5+ was able to protect components of the mitochondrial electron transport chain from peroxynitrite-mediated damage. Our study complements their data in showing, for the first time that μM mitochondrial concentrations of MnIIITE-2-PyP5+ are obtainable in vivo. For this study we have developed a new and sensitive method for MnIIITE-2-PyP5+ determination in tissues. The method is based on the exchange of porphyrin Mn2+ with Zn2+, followed by the HPLC/fluorescence detection of ZnIITE-2-PyP4+. At 4 and 7 hours after a single 10 mg/kg intraperitoneal administration of MnIIITE-2-PyP5+, the mice (8 in total) were anesthesized and perfused with saline. Mitochondria were then isolated by the method of Mela and Seitz (Methods Enzymol. 1979). We found MnIIITE-2-PyP5+ localized in heart mitochondria to 2.95 ng/mg protein. Given the average value of 0.6 μL/mg protein, the calculated MnIIITE-2-PyP5+ concentration is 5.1 μM, which is sufficient to protect mitochondria from oxidative damage.

This study establishes for the first time, that MnIIITE-2-PyP5+, a highly-charged metalloporphyrin, is capable of entering mitochondria in vivo at levels sufficient to exert there its antioxidant action; such a result encourages its development as a prospective therapeutic agent.

Keywords: MnIIITE-2-PyP5+, AEOL-10113, SOD mimic targeting mitochondria, HPLC/fluorescence detection of Mn porphyrin in vivo, heart mitochondria, Mn porphyrin/Zn porphyrin exchange

Introduction

Due to the key role of mitochondria in health and diseases, compounds able to enter the mitochondria were actively sought [1–4]. Murphy’s group has been developing mitochondria-targeted ubiquinones [1,2]. These compounds have a lipophilic triphenylphosphonium cation attached to coenzyme Q by the way of an alkyl linker. Kalyanaraman’s group showed that carboxyproxyl nitroxide linked to triphenylphosphonium ion can inhibit peroxide-induced oxidative damage and apoptosis [3]. More recently Asayama et al [4] prepared a MnIIITM-4-PyP5+ derivatized with mitochondrial targetting peptide.

Since it was designed [5], MnTE-2-PyP5+ has been extensively studied in vitro [5–18], and successfully utilized in animal models of different diseases [19–29]. Its high efficacy arises from its favorable, biologically compatible metal-centered redox potential (E1/2 = +228 mV vs NHE). Such a potential, which is similar to the potential of superoxide dismutases, allows it to perform both steps of the catalysis of O2− dismutation at nearly identical, high rates [8]. This positive potential is predominantly due to the presence of the positively charged ortho pyridyl nitrogens that exert a strong electron-withdrawing effect upon the Mn. In addition, the ortho positive charges (forming a funnel) provide electrostatic facilitation for the reaction of MnTE-2-PyP5+ with negatively charged reactive species such as O2−, ONOO− and CO3− [11]. We have shown that a monocationic parent Mn(III) porphyrin, MnIIIBr8T-2-PyP+, possessing identical E1/2 as MnIIITE-2-PyP5+, is more than 100-fold less potent a catalyst of O2− dismutation [11]. The ability of MnTE-2-PyP5+ to dismute O2− parallels its ability to scavenge ONOO− and CO3− [10,15]. As a consequence of highly positive E1/2 for MnIIIP/MnIIP redox couple, MnIIITE-2-PyP5+ is easily reducible by low-molecular weight cellular reductants such as ascorbic acid, tetrahydrobiopterin and glutathione [5]. Thus scavenging of reactive species by MnIIITE-2-PyP5+ is likely to be coupled to cellular reductants.

Although essential for its action, the multiply cationic nature of MnTE-2-PyP5+ may decrease its distribution within the cell and its organelles. Recently, Ferrer-Sueta et al have elegantly shown with submitochondrial particles that ≥ 3 μM MnIIITE-2-PyP5+ is preferable to other Mn(III) porphyrins such as MnIIITM-4-PyP5+ and MnIIITBAP3−, due to its easy reducibility by Complex I and Complex II of the mitochondrial electron transport chain, as well as by flavoenzymes such as xanthine oxidase and glucose oxidase [14]. The reduced porphyrin, MnIITE-2-PyP4+ in turn effectively reduces peroxynitrite, superoxide and carbonate radical [14]. The catalytic cycle of MnIIITE-2-PyP5+ protects not only Complex II but also other components of the mitochondrial electron transport chain [14]. Our study was intended to complement the work of Ferrer-Sueta et al [14] by showing that mitochondrial micromolar levels of MnIIITE-2-PyP5+ are attainable in vivo. Such a finding justifies further optimization of these compounds as potential therapeutics.

Thus far no sensitive method for the in vivo detection of Mn porphyrins has been reported. The HPLC/uv/vis method used for the in vivo determination of the anionic porphyrin, MnIIITBAP3− (also known MnIIITCPP3−) is not sensitive enough [30,31]. We have previously developed a HPLC/uv/vis method for the separation of atropoisomers of cationic porphyrins, H2Talkyl-2-PyP4+ and its Zn and Mn complexes, (alkyl being methyl, ethyl butyl and hexyl) from aqueous solutions [32]. Using 1H NMR and X-ray we were able to identify the individual atropoisomers (αααα, αααβ, ααββ and αβαβ) separated by HPLC [32]. Yet, uv/vis detection is not sensitive enough for the low in vivo levels of porphyrins. For this study we have developed a very sensitive HPLC/fluorescence method which is based on the exchange of the porphyrin Mn2+ site with Zn2+, followed by the fluorescence detection of ZnIITE-2-PyP4+.

Experimental - General

Porphyrins

MnIIITE-2-PyP5+ (454 nm, log ε = 5.14) [5], and ZnTE-2-PyP5+ (425.5nm, log ε=5.46) [33] were prepared as described previously.

ZnIITnBu-2-PyP4+ was used as an internal standard and was prepared as was its ethyl analogue, ZnTE-2-PyP4+. Elemental analysis for ZnIITnBu-2-PyPCl4 × 12.5 H2O: Calculated: C, 52.65; H, 6.70; N, 8.77; Cl, 11.10. Found: C, 52.65; C; H, 6.07; N, 8.76; Cl, 11.21. The log values of molar absorptivities of ZnIITnBu-2-PyP5+, were 4.46 (263.5 nm); 4.52 (327.0 nm), 5.64 (426.0 nm), 4.43 (557.0 nm) and 3.88 (593.5 nm).

Sodium L-ascorbate, mannitol, bovine serum albumin (BSA), sucrose and ethyleneglycol-bis(-aminoethylether)-N′, N, N′, N′-tetraacetic acid (EGTA) and ZnSO4 × 7 H2O were from Sigma and Zn(CH3COO)2 × 2 H2O from J. T. Baker. Acetonitrile and trifluoroacetic acid (TFA) were from Fisher Scientific and triethylamine from Pierce. Methanol (anhydrous, absolute) was from Mallinckrodt. Glacial acetic acid was from EM Science. Phosphate-buffered saline (50 mM Na phosphate, 0.9% NaCl, pH 7.4) (PBS) was from Gibco. Anti-MnSOD was from Upstate, Lake Placid, NY, anti-Lamin A from Santa Cruz, CA, and anti-β-actin from Sigma, St. Louis, MO.

Uv/vis spectroscopy

Uv/vis was done on a Shimadzu 2501 PC UV/Vis spectrophotometer.

HPLC

Equipment: Waters 2695 HPLC system (pump, autosampler, column oven) and a Waters, model 2475 fluorescence detector set on Gain 100, λexc =425 nm and λabs = 656 nm [34–36]. Column: YMC-Pack, ODS-AM, C18 column (3 μm particle size, 120 A pore size, 150 × 4.6 mm) at 45°C. Elution gradient at 1.5 mL/min: 0–15–20 min, 100% A - 80% A - 100% A, followed by 5 min column conditioning. Solvent A: 95% aqueous (deionized water, 20 mM triethylamine, pH 2.7 adjusted with concentrated TFA) and 5% acetonitrile. Solvent B: acetonitrile. Autosampler temperature: 4°C. Injection volume: 80 μL.

Methods

Transformation of the MnIIITE-2-PyP5+ into its fluorescent form

Mn(III) porphyrins are non-fluorescent [37]. Yet when the Mn3+ is replaced by a redox inactive metal, such as zinc, the metalloporphyrin becomes fluorescent [33]. This fact was used as a basis in the development of a highly sensitive method for the detection of minute quantities of MnTE-2-PyP5+ in the mice heart mitochondria homogenates.

Optimization of the Mn2+ to Zn2+ metal exchange

The MnIIITE-2-PyP5+ is a stable complex, and even in 98% sulfuric acid no observable loss of Mn occured within 24 hours [16]. However, the reduced Mn(II) porphyrin is a labile complex, and in the presence of excess zinc a metal exchange occurs leading to the formation of ZnII TE-2-PyP4+ (Scheme I). The pH most favorable for this exchange was 6.2. Lower pH causes the protonation of ascorbic acid (pKa = 4.04 [38]), and thus slows the reduction of Mn3+ to Mn2+. It also causes the demetallation of the Zn porphyrin [39]. Higher pH causes the precipitation of Zn hydroxo species (pKa=10.6 for the ZnII(H2O)22+⇒ZnII(H2O)(OH)+ + H+) [40]. Therefore, the fastest exchange and best chromatography were obtained in acetonitrile-free HPLC solvent A whose acidity was adjusted with diluted trifluoroacetic acid to pH 6.2. The exchange was significantly faster with Zn acetate than with Zn sulfate. Briefly, the 6 μM MnIIITE-2-PyP5+ was reduced aerobically by 8.3 mM ascorbate to MnIITE-2-PyP4+ in acetonitrile-free solvent A, pH 6.2, as followed by the Soret band shift from 454 nm to 438 nm [41]. Subsequently, 0.16 M Zn acetate was added and the metal exchange was followed on a Shimadzu 2501 PC UV/Vis spectrophotometer as the disappearance of MnIITE-2-PyP4+ Soret band at 438 nm, and appearance of 425.5 nm ZnIITE-2-PyP4+ Soret band [33] (Figure 1). The exchange was completed within either 14 hours at 25°C or 1 hr at 50°C.

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The spectral change associated with MnIIIP reduction, followed by Zn2+ for Mn2+ exchange at 6 μM total porphyrin concentration, 8.3 mM ascorbic acid, and 0.16 M Zn acetate in acetonitrile-free HPLC solvent A, pH 6.2, 25°C.

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The exchange of porphyrin Mn2+ with Zn2+, under conditions shown below, was used as a basis for the HPLC/fluorometric method for the determination of MnTE-2-PyP5+ levels in vivo.

MnIIITE-2-PyP5+- treatment/heart mitochondria isolation

The University of Kentucky Medical Center Research Animal Facility has a continuously accredited program from AAALAC International. All experiments using animals were performed according to the approved protocol for humane care and use of animals. Eleven C57BL/6 mice were used for the study. Three animals were injected with saline only. Eight mice were injected intraperitoneally with 10 mg/kg of MnTE-2-PyP5+ in saline. This dose was chosen based on a number of in vivo experiments where this and similar doses were used [21,22,25,26]. The mice weighted from 20 to 25 g; thus the volumes of porphyrin solution or saline injected ranged accordingly from 200 to 250 μL. Two animals were euthanatized with high-dose pentobarbital at 4 hours, and another nine animals at 7 hours after the injection of either porphyrin or saline. Before harvesting tissue, the animals were perfused with saline to avoid artifacts related to the retention of blood in the heart.

Heart mitochondria was isolated as described previously by Mela and Seitz [42,43]. Briefly, the hearts were collected, rinsed in ice-cold isolation buffer (0.225 M manitol, 0.075 M sucrose, 1 mM EGTA, pH 7.4), and cut into small pieces. The heart tissue was washed three times with the isolation buffer to remove any residual blood, and was homogenized at 500 rpm with a chilled Teflon pestle in a glass cylinder with ten strokes. The homogenate was centrifuged at 480×g at 4°C for 5 min in a Sorval SS 34 rotor. The resulting supernatant was filtered through a double-layered cheesecloth, and was centrifuged at 7700×g at 4°C for 10 min. Supernatant was saved to check for leakage from mitochondria using MnSOD, a mitochondrial matrix enzyme, as an indicator by Western blotting. The pellet was rinsed with 0.5 mL of the isolation buffer with gentle shaking to remove the “fluffy layer” (damaged mitochondria) on top of the pellet. The wall of the centrifuge tube was cleaned with cotton swabs to remove lipids. The pellet was washed by gentle re-suspension in 3 mL isolation buffer using the smooth surface of a glass rod, and centrifuged at 7700×g at 4°C for 10 min. The supernatant was saved to again check for leakage from the mitochondria. The washing was repeated once more. The resulting mitochondria were collected for further analysis. The purity of mitochondria was examined using Lamin A (a nuclear protein) and β-actin (a cytoskeletal protein) as indicators by Western blotting and is shown in Figure 2. The protein levels were determined by colorimetric assay (Bio-Rad, Richmond, CA).

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Integrity and purity of isolated mitochondria. Mitochondria were purified by centrifuging heart homogenate on a mannitol-sucrose gradient twice. Western blot probing for Lamin A (a nuclear protein) and β-actin (a cytoskeletal protein) indicated minimum contamination from non-mitochondrial fractions, and Western blot probing against MnSOD indicated there was no leaking of the purified mitochondria. Lane 1. Supernatant from centrifugation of whole heart homogenate; Lane 2. Supernatant from first washing; Lane 3. Supernatant from second washing; Lane 4. Purified mitochondria.

MnIIITE-2-PyP5+ extraction/analysis

Heart mitochondrial homogenate (100 μL) was transferred into a 2 mL polypropylene screw-cap vial. Then, 200 μL of deionized water and 300 μL of 1% acetic acid in methanol were added and mixed by vortexing for 30 sec. After incubation for 30 min and again vortexing for 30 s, the homogenate was centrifuged 5 min at 16,000 g to separate proteins. The 400 μL of the supernatant was pipetted into a 5 mL polypropylene tube (10 × 50 mm). Solvent was completely removed in a Savant Speed-Vac evaporator at 40°C within 1 h. The dry residue was dissolved in a 100 μL of deionized water containing 20 mM triethylamine, the acidity of which was adjusted with diluted TFA to pH 6.2, followed by two cycles of 30 sec vortexing and centrifugation for 2 min at 2000 g. 80 μL of the supernatant was transferred into a 2 mL polypropylene screw-cap tube, and 30 μL of 1.0 M Zn acetate in water and 10 μL of freshly prepared 0.11 M sodium ascorbate in water were added. The solution was left either overnight at 25°C or for one hour at 50°C. Then 20 μL of 2.7 M TFA and 20 μL of 100 nM ZnIITnBu-2-PyP4+ were added, followed by vortexing for 30 sec and centrifugation for 5 min at 16,000 g. The supernatant (110 μL) was transferred to an HPLC autosampler polypropylene vial equipped with a silicone/PTFE septum.

All four atropoisomers of ZnIITE-2-PyP5+ were present in the chromatogram at the abundance ratio reported previously [32] (Figure 3). ZnIITnBu-2-PyP4+ was used as an internal standard, and its atropisomers were also present in the chromatogram at the expected abundance ratio (Figure 3) [32]. The assignment of the individual atropoisomers, αααα, αααβ, ααββ and αβαβ, of both Zn porphyrins was done based on our previous HPLC/1H NMR/X-ray study [32].

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The representative HPLC chromatogram of 33.3 nM ZnIITE-2-PyP4+. The 37.5 nM ZnIITnBu-2-PyP4+ was the internal standard. The individual atropoisomers were assigned based on our previous HPLC/1H NMR/X-ray study [32]. The “α”denotes an N-alkyl above the porphyrin plane, and “β” below the plane [32].

Calibration curve

A set of serially diluted standard samples of MnIIITE-2-PyP5+ from 1.25 ng/mL to100 ng/mL in either mitochondrial homogenate that had 3 mg protein/mL (Figure 4), or in 3 mg BSA/mL PBS (Figure 4, inset) was used to construct the calibration curve. With BSA/PBS the internal standard, ZnTnBu-2-PyP4+ was added at 375 nM concentration, while with mitochondrial homogenate 10-fold less ZnTnBu-2-PyP4+ (37.5 nM) was used, giving rise to a 10-fold difference in response. Response was calculated as the ratio between standard peak area/internal standard peak area.

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Calibration curves for the determination of MnTE-2-PyP5+ levels in vivo. The curves were prepared by diluting MnTE-2-PyP5+ into either mitochondrial homogenate or into BSA/PBS (inset) whose protein concentration was 3mg/mL homogenate. With BSA/PBS the internal standard was added at 375 nM concentration, while with mitochondrial homogenate 10-fold less ZnTnBu-2-PyP4+ (37.5 nM) was used. Thus there is a 10-fold difference in otherwise identical slopes (0.00186 and 0.0191). BSA/PBS can be therefore used instead of mitochondrial homogenate, as a less costly alternative calibration medium for determination of Mn porphyrin levels in vivo.

We compared curves obtained when using either αααβ isomer (most abundant) peak area or total area under peaks of all 4 isomers and obtained identical slopes. However, by using only αααβ peak our lowest limit of quantification (LLD) is better because quantification of the least abundant αβαβ isomer at those concentration values is not possible (LLD would be limited by the area of the least abundant isomer). In our experience [32] we do not see changes in atropo-isomer abundance distribution after administration/extraction of the compound to/from animals.

Recovery of MnTE-2-PyP5+ (the overall efficacy of extraction from mitochondria plus Mn to Zn exchange) was 98 %, and was determined in the following way. A known amount of MnTE-2-PyP5+ was added to mitochondrial homogenate (3mg/mL protein), and the procedure of extraction/metal exchange was followed. The response from this experiment was compared to the response of the sample where corresponding amount of ZnTE-2-PyP4+ (equal to 100% yield of MnTE-2-PyP5+) was diluted into mobile phase.

Results and Discussion

Mitochondria are thought to be the major source of intracellular reactive species under normal and several pathological conditions. Thus injury to mitochondria contributes to a number of human pathologies. Not surprisingly, therapeutics targeting mitochondria have been intensively sought.

MnIIITE-2-PyP5+ and its mode of action/s

Based on structure-activity relationships between the catalytic rate constant for O2− dismutation and the E1/2 for the MIIIP/MIIP redox couple [5], we have developed several potent catalytic Mn porphyrin-based antioxidants, MnIIITE-2-PyP5+ being the best characterized. We have shown that MnIIITE-2-PyP5+ is remarkably effective both in vitro [5–18] and in vivo [19–29] as a consequence of its several readily accessible oxidation states (+2, +3, +4 and +5) [5,15,17]. It catalytically dismutes superoxide with log kcat of 7.76 [5], whereas the log kcat for SOD enzyme is between 9.3 and 8.84 [44–49]. Due to the ready reducibility of MnIIITE-2-PyP5+, the elimination of superoxide is likely coupled to the reduction of MnIIITE-2-PyP5+ with cellular reductants [15,17]. Radi’s group studied the peroxynitrite-related chemistry of MnIIITE-2-PyP5+ showing that it is among the fastest reductants for peroxynitrite and for carbonate radical [10,14,15]. The elimination of peroxynitrite is coupled to the reduction of both MnIIITE-2-PyP5+ and O=MnIVTE-2-PyP4+ by cellular reductants [15]. Given the rapid reaction between nitric oxide and superoxide (k = 2 × 1010 M−1s−1) [50], it is highly likely that elimination of peroxynitrite may be the predominant mode of action of MnIIITE-2-PyP5+ [14,15,51].

Since the observation that μM MnIIITE-2-PyP5+ fully protects SOD-deficient Escherichia coli against aerobic inhibition of growth [5,19], the compound has been successfully used in in vivo studies where oxidative stress is a putative factor [20–28). The most remarkable data were obtained on cancer [20,21], radioprotection [25], and diabetes [22,26,52,53]. Recent data suggest that MnIIITE-2-PyP5+ affects signaling pathways through inactivation of transcription factors such as AP-1 [20], HIF-1 [21], and NF-κB [29,52,53]. Two different mechanisms seem to be involved. The first relates to the ability of MnIIITE-2-PyP5+ to redox-modulate signaling pathways through decreasing levels or reactive oxygen and nitrogen species involved in the activation of transcription factors [20,21]. The second mechanism relates to the inhibition of NF-κB, by oxidation of exposed cysteine thiol groups on its p50 subunit upon translocation into the nucleus [52,53]. Based on the results of Ferrer-Sueta et al O=MnIVTE-2-PyP4+, formed from the oxidation of MnIIITE-2-PyP5+ by peroxynitrite (or less efficiently by H2O2), can in turn rapidly oxidize glutathione [15,17] and thus presumably protein cysteines as well. It is likely that both mechanisms may occur in parallel.

Recently, Ferrer-Sueta et al have shown, with submitochondrial particles, that ≥ 3 μM MnIIITE-2-PyP5+ protects peroxynitrite, superoxide, or carbonate radical-sensitive targets in mitochondria, while utilizing complexes I and II of mitochondrial electron transport with NADH or succinate as substrates [14]. This study is intended to complement their research by showing that despite significant hydrophilicity as a result of its high positive charge, which is essential for its antioxidant potency, MnIIITE-2-PyP5+ is indeed able to get into the mouse heart mitochondria, following a single intraperitoneal administration, and at levels high enough to protect mitochondrial respiration from oxidative damage.

In vivo detection of MnIIITE-2-PyP5+

Despite the efficacy of MnTE-2-PyP5+ in a number of animal studies, a sensitive method for its in vivo determination has been lacking. Studies, indicating the inhibition of transcription factors [20,21,29,52], the mimicking of MnSOD [20], and the oxidation of p50 subunit of NF-κB [52], imply that MnIIITE-2-PyP5+ distributes within the cell interior, and presumably into organelles as well. For the purpose of this work we have developed a new and sensitive method based on the reduction of MnIIITE-2-PyP5+ by ascorbate, followed by the exchange of Mn2+ with Zn2+, followed by HPLC/fluorescence detection of ZnIITE-2-PyP4+ (Scheme I, Figure 1). Given the high fluorescence of ZnIITE-2-PyP4+, we were able to detect porphyrin levels as low as 0.5 ng/mg of protein. Calibration curves obtained by either diluting MnTE-2-PyP5+ into mitochondrial homogenate (Figure 4), or into BSA/PBS (Figure 4, inset) were linear in the range from 1.25 (+/− 3%) to 100 (+/− 1%) ng/mL of homogenate. There was a 10-fold difference in otherwise essentially identical slopes due to the 10-fold difference in the amount of internal standard used (0.00186 with BSA/PBS and 0.0191 with mitochondrial homogenate) (Figure 4). Thus BSA/PBS can be used instead of mitochondrial homogenate as a valid and more convenient alternative calibration medium for Mn porphyrin determination.

The ortho isomers of MnIIITE-2-PyP5+, ZnIITE-2-PyP4+ and their parent metal-free ligand, H2TE-2-PyP4+ have atropoisomers, which we have previously characterized by HPLC/uv/vis/NMR and X-ray methods [32]. We observed that the abundance ratio of four isomers of ZnIITE-2-PyP4+ and their retention times on HPLC were the same in processed heart homogenates or in aqueous solution [32], indicating the absence of strong interactions of any of the four atropoisomers with cellular components (Figure 3 and ref 32). Our data also imply that the Mn porphyrin does not undergo oxidative degradation or any other modification in vivo. The method is suitable for the analysis of a variety of biological samples [54]. It may further be useful for the studies of other cationic Mn(III) porphyrins that we have been developing [8]. We are currently suing the method for the ongoing pharmacokinetic study of MnTE-2-PyP5+ in mice.

MnIIITE-2-PyP5+ levels in mitochondria

Our data show that MnIIITE-2-PyP5+ localizes in mouse heart mitochondria after a single 10 mg/kg intraperitoneal dose. The (2.95 ± 0.56) ng/mg protein of MnIIITE-2-PyP5+ were found (Table 1). The same levels were obtained at 4 or 7 hours after the administration. The mitochondrial volume reported elsewhere varied greatly from essentially being non-existent [55,56] to as much as 1.2 μL/mg protein [55–62]. (The upper limit of 1.2 μL/mg protein was previously utilized by Radi et al [63] and Quijano et al [64] to calculate concentrations of mitochondrial MnSOD and cytochrome c to be 20 μM and 400 μM, respectively). Based on an average value of mitochondrial volume of 0.6 μL/mg protein, the calculated MnIIITE-2-PyP5+ concentration in mitochondria is 5.1 μM. Ferrer-Sueta et al have shown that MnTE-2-PyP5+ was able to divert peroxynitrite from inactivation of succinate dehydrogenase and succinate oxidase equally efficiently at 3 μM (81%), 5 μM (85%) or 10 μM (83%), but not at 1 μM (28%) [14]. Thus based on their data and our findings, the 5.1 μM concentration of MnTE-2-PyP5+, achieved in mitochondria after single administration is high enough to protect mitochondrial respiration against peroxynitrite-mediated oxidative damage [5,10,14,15]. Additionally, at such levels MnTE-2-PyP5+ can compete for ONOO− with CO2, and can additionally intercept a substantial amount of CO3.−.

Table 1

The levels of MnIIITE-2-PyP5+ in C57BL/6 mouse heart mitochondria. The mean value was calculated to be (2.95 ± 0.56) ng/mg protein.

Mousedrug10 mg/kg i.p.total protein mg/mL homogenateMnIIITE-2-PyP5+ ng/mL homogenateMnIIITE-2-PyP5+ ng/mg protein
Mice were sacrificed 7 hours after drug administration
1MnIIITE-2-PyP5+2.8206.552.32
2MnIIITE-2-PyP5+2.5436.752.65
3MnIIITE-2-PyP5+2.6827.822.91
4MnIIITE-2-PyP5+2.8338.152.88
5MnIIITE-2-PyP5+1.7943.832.13
6MnIIITE-2-PyP5+1.8247.173.93
Mice were sacrificed 4 hours after drug administration
7MnIIITE-2-PyP5+1.2234.283.50
8MnIIITE-2-PyP5+1.9096.293.29
Control mice
9saline3.1470.000.00
10saline3.1930.000.00
11saline2.9400.000.00

This work answers affirmatively an important question as to whether MnIIITE-2-PyP5+ and similar, highly-charged metalloporphyrins are capable of entering mitochondrion at levels high enough to exert there their presumed antioxidant action. Moreover it indicates that having been taken into mitochondria in vivo the Mn porphyrin resists washing out during isolation of the mitochondria.

Conclusions

The new and sensitive method developed herein enables us to show that, despite its hydrophilicity, i.e. overall high positive charge, which is essential for its in vivo antioxidant efficacy, MnIIITE-2-PyP5+ targets mitochondria after only single dose of 10 mg/kg, achieving micromolar levels that are sufficient to exert protection of the mitochondrial respiration from oxidative damage. Therefore, along with the report of Ferrer-Sueta et al [14] this study justifies further improvement of Mn(III) porphyrins as therapeutics for protecting mitochondria from oxidative damage.

Acknowledgments

Ivan Spasojeviæ acknowledges NIH/NCI Duke Comprehensive Cancer Center Core Grant (5-P30-CA14236-29). Ines Batini -Haberle appreciates financial support from NIH- IR21-ESO/3682, W19A167798-01, and NIH U19 AI67798-01. Yumin Chen, Marsha Cole, Yunfeng Zhao, Teresa Noel and Daret St. Clair are thankful to the support of NIH grants CA 49797, CA 73599 and CA 94853. Authors are also thankful to Rafael Radi and Gerardo Ferrer-Sueta for helpful discussions and to Irwin Fridovich for critical reading of the manuscript and for his continuous support.

Abbreviations

SOD
superoxide dismutase
NHE
normal hydrogen electrode
MnP
any Mn(III) porphyrin
para isomer
MnIIITM-4-PyP5+, Mn(III) meso-tetrakis(N-methylpyridinium-4-yl)porphyrin
ortho isomer
MnIIITE-2-PyP5+, Mn(III) meso-tetrakis(N-ethylpyridinium-2-yl)porphyrin (AEOL-10113)
MnIIITBAP3−(also known as MnTCPP3−)
Mn(III) meso-tetrakis(4-carboxylatophenyl)porphyrin
ZnIITE-2-PyP4+
Zn meso-tetrakis(N-ethylpyridinium-2-yl)porphyrin
ZnIITnBu-2-PyP4+
Zn meso-tetrakis(N-n-butylpyridinium-2-yl)porphyrin
H2Talkyl-2-PyP4+meso-tetrakis(N-alkylpyridinium-2-yl)porphyrin
alkyl being methyl (M), ethyl (E), n-butyl (nBu) and n-hexyl (nHex)
meso
is indicating substitution in 5,10,15,20 positions on porphyrin core
HIF-1
hypoxia inducible factor-1,
NF-κB
nuclear factor -κB
AP-1
activator protein-1
BSA
bovine serum albumine
TFA
trifluoroacetic acid
PBS
phosphate-buffered saline

Footnotes

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